Total Synthesis of (+)-Raputindole A: An Iridium-Catalyzed Cyclization Approach
Author:
Affiliation:
1. Institute of Chemistry, University of São Paulo (USP), 05508-000 São Paulo, São Paulo, Brazil
2. Institute of Chemistry, University of Campinas, 13083-970 Campinas, São Paulo, Brazil
Funder
Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c01943
Reference30 articles.
1. The Raputindoles: Novel Cyclopentyl Bisindole Alkaloids from Raputia simulans
2. Prenylindole alkaloids from Raputia praetermissa (Rutaceae) and their chemosystematic significance
3. Total Synthesis of (+)-trans-Trikentrin A
4. A practical, multi-gram synthesis of (±)-herbindole A, (±)-herbindole B, and (±)-herbindole C from a common intermediate via 6,7-indole aryne cycloaddition and Pd(0)-catalyzed cross-coupling reactions
5. Shearinines D–K, new indole triterpenoids from an endophytic Penicillium sp. (strain HKI0459) with blocking activity on large-conductance calcium-activated potassium channels
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